Modulation of gene expression and inflammation but not DNA damage after sevoflurane anesthesia

IF 2.3 4区 医学 Q3 ENVIRONMENTAL SCIENCES
Mariane A. P. Silva, Leandro G. Braz, José Reinaldo C. Braz, Mariana G. Braz
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引用次数: 0

Abstract

This study assessed, for the first time, the expression of the genes hOGG1, TP53, and IL-6 in leukocytes by real-time quantitative polymerase chain reaction in surgical patients before (baseline), during (2 h of anesthesia) and 1 day after sevoflurane anesthesia. Additionally, DNA damage was detected by the comet assay, serum interleukin (IL)-6 was detected by flow cytometry, and differential leukocyte counting was also performed. TP53 and hOGG1 expression was downregulated on the day after anesthesia compared to before anesthesia. However, IL-6 expression did not change, and no DNA damage induction was observed during or after anesthesia. At the systemic level, mild neutrophilia and an increase in IL-6 levels occurred after anesthesia. Our findings suggest that sevoflurane anesthesia downregulates gene expression (hOGG1 and TP53) and contributes to an inflammatory status (increased systemic IL-6 and mild neutrophilia) but is not associated with DNA damage in patients without comorbidities who undergo minor elective surgery.

七氟醚麻醉后基因表达和炎症的调节,而非DNA损伤
本研究首次采用实时定量聚合酶链反应技术,对手术患者在麻醉前(基线)、麻醉中(2小时)和七氟醚麻醉后1天白细胞中hOGG1、TP53和IL-6基因的表达进行了评估。此外,用彗星法检测DNA损伤,用流式细胞术检测血清白细胞介素(IL)-6,并进行白细胞鉴别计数。与麻醉前相比,麻醉后1天TP53和hOGG1表达下调。然而,IL-6的表达没有改变,麻醉期间和麻醉后没有观察到DNA损伤的诱导。在全身水平,麻醉后出现轻度中性粒细胞增多和IL-6水平升高。我们的研究结果表明,七氟醚麻醉下调基因表达(hOGG1和TP53),并有助于炎症状态(全身IL-6增加和轻度中性粒细胞增多),但与接受小选择性手术的无合共病患者的DNA损伤无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.40
自引率
10.70%
发文量
52
审稿时长
12-24 weeks
期刊介绍: Environmental and Molecular Mutagenesis publishes original research manuscripts, reviews and commentaries on topics related to six general areas, with an emphasis on subject matter most suited for the readership of EMM as outlined below. The journal is intended for investigators in fields such as molecular biology, biochemistry, microbiology, genetics and epigenetics, genomics and epigenomics, cancer research, neurobiology, heritable mutation, radiation biology, toxicology, and molecular & environmental epidemiology.
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